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An assembly factor promotes assembly of flavinated SDH1 into the succinate dehydrogenase complex

Belt, Katharina ; Van Aken, Olivier LU ; Murcha, Monika ; Millar, A. Harvey and Huang, Shaobai (2018) In Plant Physiology 177(4). p.1439-1452
Abstract

Succinate dehydrogenase (Complex II; SDH) plays an important role in mitochondrial respiratory metabolism. The SDH complex consists of four core subunits and multiple cofactors, which must be assembled correctly to ensure enzyme function. To date, only an assembly factor (SDHAF2) required for FAD insertion into subunit SDH1 has been identified in plants. Here, we report the identification of Arabidopsis (Arabidopsis thaliana) At5g67490 as a second SDH assembly factor. Knockout of At5g67490 (sdhaf4) did not cause any phenotypic variation in seedlings but resulted in a decrease in both SDH activity and the succinate-dependent respiration rate as well as increased accumulation of succinate. Mass spectrometry analyses revealed stable levels... (More)

Succinate dehydrogenase (Complex II; SDH) plays an important role in mitochondrial respiratory metabolism. The SDH complex consists of four core subunits and multiple cofactors, which must be assembled correctly to ensure enzyme function. To date, only an assembly factor (SDHAF2) required for FAD insertion into subunit SDH1 has been identified in plants. Here, we report the identification of Arabidopsis (Arabidopsis thaliana) At5g67490 as a second SDH assembly factor. Knockout of At5g67490 (sdhaf4) did not cause any phenotypic variation in seedlings but resulted in a decrease in both SDH activity and the succinate-dependent respiration rate as well as increased accumulation of succinate. Mass spectrometry analyses revealed stable levels of FAD-SDH1 in sdhaf4, together with increased levels of the FAD-SDH1 assembly factor, SDHAF2, and reduced levels of SDH2 compared with the wild type. Loss of SDHAF4 in sdhaf4 inhibited the formation of the SDH1/SDH2 intermediate, leading to the accumulation of soluble SDH1 in the mitochondrial matrix and reduced levels of SDH1 in the membrane. The increased levels of SDHAF2 suggest that the stabilization of soluble FAD-SDH1 depends on SDHAF2 availability. We conclude that SDHAF4 acts on FAD-SDH1 and promotes its assembly with SDH2, thereby stabilizing SDH2 and enabling its full assembly with SDH3/ SDH4 to form the SDH complex.

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author
organization
publishing date
type
Contribution to journal
publication status
published
subject
in
Plant Physiology
volume
177
issue
4
pages
14 pages
publisher
American Society of Plant Biologists
external identifiers
  • pmid:29930107
  • scopus:85060520223
ISSN
0032-0889
DOI
10.1104/pp.18.00320
language
English
LU publication?
yes
id
734c9717-1321-4cbf-8f19-74b4acbc2dce
date added to LUP
2019-02-08 12:28:36
date last changed
2020-07-08 04:41:35
@article{734c9717-1321-4cbf-8f19-74b4acbc2dce,
  abstract     = {<p>Succinate dehydrogenase (Complex II; SDH) plays an important role in mitochondrial respiratory metabolism. The SDH complex consists of four core subunits and multiple cofactors, which must be assembled correctly to ensure enzyme function. To date, only an assembly factor (SDHAF2) required for FAD insertion into subunit SDH1 has been identified in plants. Here, we report the identification of Arabidopsis (Arabidopsis thaliana) At5g67490 as a second SDH assembly factor. Knockout of At5g67490 (sdhaf4) did not cause any phenotypic variation in seedlings but resulted in a decrease in both SDH activity and the succinate-dependent respiration rate as well as increased accumulation of succinate. Mass spectrometry analyses revealed stable levels of FAD-SDH1 in sdhaf4, together with increased levels of the FAD-SDH1 assembly factor, SDHAF2, and reduced levels of SDH2 compared with the wild type. Loss of SDHAF4 in sdhaf4 inhibited the formation of the SDH1/SDH2 intermediate, leading to the accumulation of soluble SDH1 in the mitochondrial matrix and reduced levels of SDH1 in the membrane. The increased levels of SDHAF2 suggest that the stabilization of soluble FAD-SDH1 depends on SDHAF2 availability. We conclude that SDHAF4 acts on FAD-SDH1 and promotes its assembly with SDH2, thereby stabilizing SDH2 and enabling its full assembly with SDH3/ SDH4 to form the SDH complex.</p>},
  author       = {Belt, Katharina and Van Aken, Olivier and Murcha, Monika and Millar, A. Harvey and Huang, Shaobai},
  issn         = {0032-0889},
  language     = {eng},
  number       = {4},
  pages        = {1439--1452},
  publisher    = {American Society of Plant Biologists},
  series       = {Plant Physiology},
  title        = {An assembly factor promotes assembly of flavinated SDH1 into the succinate dehydrogenase complex},
  url          = {http://dx.doi.org/10.1104/pp.18.00320},
  doi          = {10.1104/pp.18.00320},
  volume       = {177},
  year         = {2018},
}